Trophic Interactions Between Astroglial Cells and Hippocampal Neurons in Culture

Growth of a rat neuroblastoma cell line in serum-free supplemented medium.

Bottenstein, J. E., & SATO, G. H. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.514 · Cited by 2,268

Rat hippocampal neurons in dispersed cell culture.

Banker, G. A., & Cowan, W. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90594-7 · Cited by 1,110

Growth and cultivation of dissociated neurons and glial cells from embryonic chick, rat and human brain in flask cultures.

Booher, J., & Sensenbrenner, M. (1972) · PubMed · Cited by 760

Adult rat brain astrocytes support survival of both NGF-dependent and NGF-insensitive neurones

Lindsay, R. M. (1979) · Nature · doi:10.1038/282080a0 · Cited by 373

Trophic Mechanisms in the Peripheral Nervous System

Varon, S. S., & Bunge, R. P. (1978) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.01.030178.001551 · Cited by 326

Further observations on hippocampal neurons in dispersed cell culture

Banker, G. A., & Cowan, W. M. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901870302 · Cited by 285

Nerve Growth Factor

Bradshaw, R. A. (1978) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.47.070178.001203 · Cited by 246

Neuron-glia interactions.

Varon, S. S., & Gg, S. (1979) · PubMed · Cited by 244

Induction of neurite outgrowth by a conditioned-medium factor bound to the culture substratum

Collins, F. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.10.5210 · Cited by 241

Survival and development in culture of dissociated parasympathetic neurons from ciliary ganglia

Helfand, S. L., Smith, G. A., & Wessells, N. K. (1976) · Developmental Biology · doi:10.1016/0012-1606(76)90174-3 · Cited by 177

Cell Biology of Glia

Steward, O. (2000) · Springer eBooks · doi:10.1007/978-1-4612-1198-3_5

Mass spectrometry-based proteomics reveals distinct mechanisms of astrocyte protein secretion

Greco, T. M. (2009) · ScholarlyCommons (University of Pennsylvania)

In vitro direct conversion of somatic cells from the adult human brain into functional neurons by defined factors

del Valle, R. S. (2013) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.15377

BDNF in developing aortic baroreceptors & its role in the dendritic morphogenesis of neurons from the Nucleus Tractus Solitarius

Martin, J. L. (2010)

Studies on microtubule nucleation during axon growth

Stieß, M. (2010) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.12357

Beta-Amyloid Precursor: A Neuronal and Glial-Derived Protein With Trophic-like Activities

Siman, R. G. (1994) · Elsevier eBooks · doi:10.1016/b978-0-08-042276-3.50025-2

Role of APC Complexes and the Microtubule Cytoskeleton in Neuronal Morphogenesis

Votin, V., Nelson, W. J., & Barth, A. I. M. (2007) · Elsevier eBooks · doi:10.1016/b978-012369437-9/50005-0

Gene therapy for neurodegenerative disorders and malignant brain tumors

Chiang, L., Flores, E. P., Wen, D. Y. K., Hall, W. A., & Low, W. C. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037316

Multiple obstacles to gene therapy in the brain

Sanders, D. A. R. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0003747x

Infusion of Glial Maturation Factor-β Reduces Behavioral Deficits After Caudate Nucleus Injury in Rats

Palatucci, C., Fülöp, Z. L., Lim, R., & Stein, D. G. (1996) · International Journal of Neuroscience · doi:10.3109/00207459608987259

Are fetal brain tissue grafts necessary for the treatment of brain damage?

Stein, D. G., & Glasier, M. M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037596

CNS transplant utility may surive even their hasty clinical application

Nieto‐Sampedro, M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037444

Therapeutic neural transplantation: Boon or boondoggle?

Haring, J. H. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037390

Pathway rewiring with neural transplantation

Strata, P., & Rossi, F. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037535

Neural transplantation, cognitive aging and speech

Lynch, M. P. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037419

The limitations of central nervous systemdirected gene transfer

Davidson, B. L. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0003733x

Transplantation, plasticity, and the aging host

Felten, D. L. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037377

The spinal cord as an alternative model for nerve tissue graft

Privat, A., & y Ribotta, M. G. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037456

Principles of brain tissue engineering

Freed, W. J., & Smith, T. D. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037389

Will brain tissue grafts become an important therapy to restore visual function in cerebrally blind patients?

Werth, R. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037559

Neural grafting in human disease versus animal models: Cautionary notes

Steece‐Collier, K. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037523

Building a rational foundation for neural transplantation

Davis, H. P., & Volpe, B. T. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037341

Elegant studies of transplant-derived repair of cognitive performance

Dunnett, S. B., & Torres, E. M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037365

Polarized sorting of the viral glycoproteins of Herpes Simplex Virus Type I in murine embryonic neurons in culture: A confocal laser scanning microscopic study

Hashimoto, I., Kimura, T., & Ohyama, A. (1994) · The Journal of Kansai Medical University · doi:10.5361/jkmu1956.46.1-2_25

Repairing the brain: Trophic factor or transplant?

Bond, N. W. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037298

Grafts and the art of mind's reconstruction

Sinden, J. D., Hodges, H., & Gray, J. A. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037584

Behavioral effects of neural grafts: Action still in search of a mechanism

Woodruff, M. L. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037560

Local and global gene therapy in the central nervous system

Muldoon, L. L., & Neuwelt, E. A. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037572

Gene therapy and neural grafting: Keeping the message switched on

Svendsen, C. N., & Dunnett, S. B. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037547

Intraretrosplenial grafts of cholinergic neurons and spatial memory function

Li, Y. J., & Low, W. C. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037407

The ethics of fetal tissue grafting should be considered along with the science

Crutcher, K. A. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037328

Gene replacement therapy in the CNS: A view from the retina

Seigel, G. M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037493

Difficulties inherent in the restoration of dynamically reactive brain systems

Stanfield, B. B. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037511

A Role for c-Jun Kinase (JNK) Signaling in Glial Engulfment of Degenerating Axons: A Dissertation

MacDonald, J. M. (2012) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/xtd8-cc59

Involvement of neuroligins and associated proteins in synapse development

Levinson, J. N. (2010) · cIRcle (University of British Columbia) · doi:10.14288/1.0071424

Astrocytes release small molecules to protect neurons from oxidative stress

Wang, X. (2009) · cIRcle (University of British Columbia) · doi:10.14288/1.0090451

Roles of Neural Stem Cells in Alcohol Use Disorders

Wagner, J. L., Barton, E. A., Geil, C., Leasure, J. L., & Nixon, K. (2015) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814623186_0010

The molecular mechanisms controlling spontaneous activity in the developing cochlea

Wang, H. C. (2015)

Repurposing Clinic-Tested Drugs to Treat Rare Neurogenetic Diseases by Transcriptional Modulation

Hadwen, J. (2018) · uO Research (University of Ottawa) · doi:10.20381/ruor-21849

Neural Tissue Transplants Modify Response of the Immature Spinal Cord to Damage

Bregman, B. S., & Reier, P. J. (1987) · Springer eBooks · doi:10.1007/978-3-642-71381-1_31

Activity-based automatic ROI generation (AARG) analysis of dendritic spine calcium transients reveals distance-dependent activity of voltage-gated calcium channels

Gilbride, C. J. (2018) · doi:10.53846/goediss-6794

Detection of Fibroblast Growth Factor Receptor 1 (FGFR1) Transactivation by Muscarinic Acetylcholine Receptors (mAChRs) in Primary Neuronal Hippocampal Cultures Through Use of Biochemical and Morphological Approaches

Liberto, V. D., Mudò, G., Borroto‐Escuela, D. O., Fuxé, K., & Belluardo, N. (2018) · Neuromethods · doi:10.1007/978-1-4939-8576-0_5

Stress effects on astrocyte communication and regulation of adult hippocampal neural stem cells

Covarrubias, D. (2015) · eScholarship (California Digital Library)

STUDY OF THE EXPRESSIONS OF IL-20R1 AND IL-20R2 IN C57BL/6 MICE ASTROGLIAL CELLS

Abd‐Nikfarjam, B., Ebtekar, M., Sabouni, F., Pourpak, Z., & Maryam, K. (2013) · Pathobiology Research

Vasoactive Intestinal Peptide and Astrocyte Mitogenesis: In Vitro and in Vivo Studies

Hill, J. M., & Brenneman, D. E. (1993) · Springer eBooks · doi:10.1007/978-1-4615-2846-3_20

Physiological consequences of astrocyte-to-neuron signaling

Sanzgiri, R. P. (1998) · doi:10.31274/rtd-180813-10807

Transplantation of stem cells from human umbilical cord blood to improve regeneration after spinal cord injury

Schira‐Heinen, J. (2011) · Univ. Duesseldorf: Duesseldorfer Dokumenten- und Publikationsserver

Faculty Opinions recommendation of Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.

Bonni, A., & Ikeuchi, Y. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1161225.621706

Cell Biology of Glia

Steward, O. (1989) · Springer eBooks · doi:10.1007/978-1-4612-3540-8_2

Trophic disorders

Appenzeller, O., Lamotte, G. J., & Coon, E. A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-96011-3.00009-7

Reactive astrocytes and glioblastoma: are there new targets for more effective antitumor therapy?

Tyagunova, E. E., Доброхотова, В. З., & Dushina, A. (2023) · Head and neck tumors (HNT) · doi:10.17650/2222-1468-2023-13-2-57-64

Autoimmune Astrocytopathy

Correale, J. D., & Marrodán, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-24297-7_10-1

Neurons in Context

Lux, V. (2024) · SpringerBriefs in psychology · doi:10.1007/978-3-031-55229-8_4

Autoimmune Astrocytopathy

Correale, J. D., & Marrodán, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-60006-7_10

Radial-glia-to-astrocyte trans-differentiation and astrocyte transcriptional convergence are coordinated by CEH-43/DLX in C. elegansPreprint

Liu, S., Bradley, K., Tang, J. J., Kim, Y. A., Milosevic, A., & Shaham, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.17.682973 · Cited by 1

Biosynthesis of all-trans-Retinoic Acid and Regulation of Retinoids Homeostasis in Primary Hippocampal Astrocytes and Neurons

Wang, C. (2010) · eScholarship (California Digital Library)

Molecular mechanisms underlying the surface organization of the NMDA receptors during development

Bénac, N. (2024) · theses.fr (ABES) · doi:10.70675/e3508a2ezb62ez4f99zb27bz156201271974

Neural changes in forelimb cortex and behavioural development

Coles, B. L. K. (1996) · Library and Archives Canada (Government of Canada)

Vasoactive Intestinal Peptide: From Molecular Genetics to Neurotropism

Gozes, I., & Brenneman, D. E. (1993) · Springer eBooks · doi:10.1007/978-1-4615-2846-3_2

Untitled work

(1999) · doi:10.1002/(sici)1098-1136(19990201)25:3

Untitled work

Melcangi (1999) · doi:10.1002/(sici)1097-4695(19990915)40:4

Untitled work

(1999) · doi:10.1002/(sici)1097-4695(19990205)38:2

Untitled work

(1998) · doi:10.1002/(sici)1096-9861(19981005)399:4

A neurotrophic factor (NTF) released from primary glial cultures supports survival and fiber outgrowth of cultured hippocampal neurons

Müller, H. W., & Seifert, W. E. (1982) · Journal of Neuroscience Research · doi:10.1002/jnr.490080209 · Cited by 179

The output of neuronotrophic and neurite-promoting agents from rat brain astroglial cells: a microculture method for screening potential regulatory molecules

Rudge, J. S., Manthorpe, M., & Varon, S. S. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90188-9 · Cited by 145

Interactions of astroglia derived factors with hippocampal neurons

Matthiessen, H. P., Schmalenbach, C., & Müller, H. W. (1987) · Journal of Neuroimmunology · doi:10.1016/0165-5728(87)90311-0

A Neuron-Astrocyte Co-Culture System to Investigate Astrocyte-Secreted Factors in Mouse Neuronal Development

Jones, E. V., Cook, D., & Murai, K. K. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-452-0_22 · Cited by 60

Divergent Trophic Actions of Glioma Conditioned Media on Cultured Rat Hippocampal Neurons.

Okuda, S., Saitō, H., & Katsuki, H. (1994) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.17.735 · Cited by 3